ClinVar Miner

List of variants reported as likely benign for 46,XY sex reversal 6 by Labcorp Genetics (formerly Invitae), Labcorp

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 62
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005921.2(MAP3K1):c.138G>A (p.Glu46=) rs1051867310 0.00049
NM_005921.2(MAP3K1):c.2598C>T (p.Ala866=) rs201679580 0.00034
NM_005921.2(MAP3K1):c.2431A>G (p.Met811Val) rs189290632 0.00026
NM_005921.2(MAP3K1):c.934A>T (p.Met312Leu) rs376808920 0.00020
NM_005921.2(MAP3K1):c.4114+10C>G rs1249749160 0.00019
NM_005921.2(MAP3K1):c.576C>T (p.Thr192=) rs372106846 0.00018
NM_005921.2(MAP3K1):c.743G>A (p.Arg248Gln) rs201579608 0.00015
NM_005921.2(MAP3K1):c.2012C>T (p.Ala671Val) rs201310278 0.00012
NM_005921.2(MAP3K1):c.2571G>A (p.Met857Ile) rs367884272 0.00011
NM_005921.2(MAP3K1):c.185T>G (p.Leu62Arg) rs1423534461 0.00007
NM_005921.2(MAP3K1):c.2479G>A (p.Val827Ile) rs763246417 0.00007
NM_005921.2(MAP3K1):c.1921A>G (p.Met641Val) rs759485701 0.00006
NM_005921.2(MAP3K1):c.3774T>C (p.Tyr1258=) rs766640051 0.00005
NM_005921.2(MAP3K1):c.917G>A (p.Arg306His) rs375262853 0.00005
NM_005921.2(MAP3K1):c.1605A>G (p.Gln535=) rs56232761 0.00003
NM_005921.2(MAP3K1):c.2617G>A (p.Val873Ile) rs149242419 0.00003
NM_005921.2(MAP3K1):c.3070A>C (p.Lys1024Gln) rs780666910 0.00003
NM_005921.2(MAP3K1):c.4107T>C (p.Asp1369=) rs373835578 0.00003
NM_005921.2(MAP3K1):c.4128A>C (p.Leu1376=) rs113150610 0.00003
NM_005921.2(MAP3K1):c.916C>T (p.Arg306Cys) rs749900834 0.00003
NM_005921.2(MAP3K1):c.959A>G (p.Gln320Arg) rs770264567 0.00003
NM_005921.2(MAP3K1):c.1035+12C>T rs773590377 0.00002
NM_005921.2(MAP3K1):c.1801G>A (p.Glu601Lys) rs761556838 0.00002
NM_005921.2(MAP3K1):c.2091C>T (p.Arg697=) rs372638992 0.00002
NM_005921.2(MAP3K1):c.3819+9C>G rs753158018 0.00002
NM_005921.2(MAP3K1):c.548G>A (p.Arg183Gln) rs1454725137 0.00002
NM_005921.2(MAP3K1):c.1015C>T (p.Arg339Trp) rs373572109 0.00001
NM_005921.2(MAP3K1):c.1613A>G (p.Asn538Ser) rs374113323 0.00001
NM_005921.2(MAP3K1):c.1782C>G (p.Ala594=) rs746154320 0.00001
NM_005921.2(MAP3K1):c.1926C>A (p.Val642=) rs867527029 0.00001
NM_005921.2(MAP3K1):c.2133A>G (p.Lys711=) rs774048753 0.00001
NM_005921.2(MAP3K1):c.3828T>C (p.Tyr1276=) rs372801625 0.00001
NM_005921.2(MAP3K1):c.3957C>T (p.Tyr1319=) rs1478914246 0.00001
NM_005921.2(MAP3K1):c.4092A>G (p.Gln1364=) rs773915109 0.00001
NM_005921.2(MAP3K1):c.4258-5T>C rs761483754 0.00001
NM_005921.2(MAP3K1):c.4304T>C (p.Val1435Ala) rs1356600233 0.00001
NM_005921.2(MAP3K1):c.597C>T (p.His199=) rs781610164 0.00001
NM_005921.2(MAP3K1):c.614G>A (p.Arg205Lys) rs768329767 0.00001
NM_005921.2(MAP3K1):c.1524T>G (p.Pro508=)
NM_005921.2(MAP3K1):c.1599G>A (p.Arg533=) rs2530928807
NM_005921.2(MAP3K1):c.1687-17GT[2]
NM_005921.2(MAP3K1):c.1758T>A (p.Arg586=)
NM_005921.2(MAP3K1):c.1803G>A (p.Glu601=)
NM_005921.2(MAP3K1):c.1846G>A (p.Gly616Arg) rs143853590
NM_005921.2(MAP3K1):c.201T>C (p.Ser67=) rs2111726323
NM_005921.2(MAP3K1):c.2241A>G (p.Glu747=)
NM_005921.2(MAP3K1):c.2370-17A>G rs2530951771
NM_005921.2(MAP3K1):c.261C>G (p.Ser87=) rs1188647175
NM_005921.2(MAP3K1):c.2696A>G (p.Asn899Ser) rs142968004
NM_005921.2(MAP3K1):c.2824ACA[4] (p.Thr946_Thr949del) rs5868032
NM_005921.2(MAP3K1):c.2824ACA[9] (p.Thr949_Glu950insThr) rs5868032
NM_005921.2(MAP3K1):c.3060A>G (p.Gln1020=)
NM_005921.2(MAP3K1):c.30G>T (p.Ser10=)
NM_005921.2(MAP3K1):c.3198C>G (p.Thr1066=) rs918712593
NM_005921.2(MAP3K1):c.347C>T (p.Ala116Val) rs1046935979
NM_005921.2(MAP3K1):c.3609C>T (p.Pro1203=) rs1554035881
NM_005921.2(MAP3K1):c.3667-4G>A rs552563402
NM_005921.2(MAP3K1):c.3846T>G (p.Ser1282=) rs375842337
NM_005921.2(MAP3K1):c.429C>T (p.Pro143=) rs1211934332
NM_005921.2(MAP3K1):c.450C>T (p.Ala150=)
NM_005921.2(MAP3K1):c.786G>T (p.Val262=) rs1382596856
NM_005921.2(MAP3K1):c.89C>A (p.Ala30Asp) rs971549264

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.